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Original Articles

Kinetic Study of an Esterification by Monitoring Pitch Changes in a Cholesteric Liquid Crystal Solvent

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Pages 9-20 | Received 18 Dec 1978, Published online: 28 Mar 2007

References

  • Elias , H G. , ed. 1977 . Polymerization of Organic Systems 117 – 173 . New York : Gordon and Breach . See for example.(,ed. by, pp.
  • Barnett , W E. and Sohn , W H. 1971 . Chem. Commun. , : 1002
  • Nerbonne , J M. and Weiss , R G. 1978 . J. Am. Chem. Soc , 100 : 2571
  • Mioskowski , C. , Candau , J B. S. and Salladie , G. 1976 . Chem. Phys. Lett. , 38 : 456
  • Bacon , W E. and Brown , G H. 1971 . Mot. Cryst. Liq. Cryst. , 12 : 229
  • Dewar , M J. S. and Nahlovsky , B D. 1974 . J. Am. Chem. Soc , 96 : 460
  • Aviv , G. , Sagiv , J. and Yogev , A. 1976 . Mol. Cryst. Liq. Cryst. , 36 : 349
  • Strzelecki , L. and Liebert , L. 1973 . Bull. Soc. Chim. France , : 597 ibid. 603 (1973); ibid. 605 (1973).
  • Park , J W. and Labes , M M. 1976 . Mol. Cryst. Liq. Cryst. Lett. , 34 : 25
  • Baessler , H. and Labes , M M. 1971 . J. Chem. Phys. , 52 : 631
  • The cholesteric solvent B was not the “best” solvent in terms of its α°/n value and its cholesteric temperature range. The largest value (α°/n = 16600) of α°/n for reaction system 1 was observed for the mixture of CN, CC, COC and PCPB (90:10:40; 150 weight ratio), which also showed the widest cholesteric temperature range (room temperature—95.6°C). However, in this solvent, the acid anhydride was not stable chemically at the reaction temperatures, judging from the gradual red shift of λmax with time. We therefore chose cholesteric solvent B as a reaction solvent primarily because of its chemical stability with both reactants and products. In this solvent, the reaction had to be carried out at temperatures above 45°C, because of the gradual crystallization of the solution at temperatures below 40°C. Reaction system I was then selected for further study, since the kinetics could be studied over a wider temperature range (45-65°C) than system V (45-58°C).
  • Fahim , H A. J. Chem. Soc , 1949 520
  • Klanderman , B H. and Criswell , T R. 1975 . J. Am. Chem. Soc , 97 : 1585
  • Klarmann , E. , Gatvas , L W. and Shternov , V A. 1932 . J. Am. Chem. Soc , 54 : 298
  • Shriner , R L. and Young , J H. 1930 . J. Am. Chem. Soc , 52 : 3332
  • Marcinkiewicz , S. , Green , J. and McHale , D. 1963 . J. Chromatoq. , 10 : 42
  • 1955 . Organic Synthesis Coll. Vol. 3 , 28
  • Adams , J E. , Haas , W. and Wysocki , J. 1969 . J. Chem. Phys. , 50 : 2458

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